CA2642921A1 - 4-phenyl-thiazole-5-carboxylic acids and 4-phenyl-thiazole-5-carboxylic acid amides as plk1 inhibitors - Google Patents

Info

Publication number

CA2642921A1

CA2642921A1 CA002642921A CA2642921A CA2642921A1 CA 2642921 A1 CA2642921 A1 CA 2642921A1 CA 002642921 A CA002642921 A CA 002642921A CA 2642921 A CA2642921 A CA 2642921A CA 2642921 A1 CA2642921 A1 CA 2642921A1

Authority

CA

Canada

Prior art keywords

thiazole

carboxylic acid

phenyl

benzoimidazol

dimethoxy

Prior art date

2006-02-27

Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)

Abandoned

Links

• Espacenet
• Global Dossier
• CIPO
• Discuss

• 239000003112 inhibitor Substances 0.000 title description 17
• NGTZFWMOTDGMKO-UHFFFAOYSA-N 4-phenyl-1,3-thiazole-5-carboxylic acid Chemical class S1C=NC(C=2C=CC=CC=2)=C1C(=O)O NGTZFWMOTDGMKO-UHFFFAOYSA-N 0.000 title description 3
• ZLKBOBCOZBUZSF-UHFFFAOYSA-N 4-phenyl-1,3-thiazole-5-carboxamide Chemical class S1C=NC(C=2C=CC=CC=2)=C1C(=O)N ZLKBOBCOZBUZSF-UHFFFAOYSA-N 0.000 title 1
• 101150073897 plk1 gene Proteins 0.000 title 1
• 150000001875 compounds Chemical class 0.000 claims abstract description 197
• 238000000034 method Methods 0.000 claims abstract description 75
• 150000003839 salts Chemical class 0.000 claims abstract description 23
• 239000000203 mixture Substances 0.000 claims description 43
• 125000000217 alkyl group Chemical group 0.000 claims description 33
• 102100031463 Serine/threonine-protein kinase PLK1 Human genes 0.000 claims description 29
• 108010056274 polo-like kinase 1 Proteins 0.000 claims description 28
• 125000000623 heterocyclic group Chemical group 0.000 claims description 27
• 229910052736 halogen Inorganic materials 0.000 claims description 23
• 229910052739 hydrogen Inorganic materials 0.000 claims description 22
• 239000001257 hydrogen Substances 0.000 claims description 21
• 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 20
• 150000002367 halogens Chemical class 0.000 claims description 18
• 125000004432 carbon atom Chemical group C* 0.000 claims description 17
• 239000000543 intermediate Substances 0.000 claims description 17
• IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 16
• 230000000694 effects Effects 0.000 claims description 16
• 125000003107 substituted aryl group Chemical group 0.000 claims description 14
• 206010028980 Neoplasm Diseases 0.000 claims description 13
• 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 12
• UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 11
• 125000003545 alkoxy group Chemical group 0.000 claims description 11
• 125000003118 aryl group Chemical group 0.000 claims description 11
• 229910052757 nitrogen Inorganic materials 0.000 claims description 11
• ASNYTHITDPHAHV-UHFFFAOYSA-N 4-(3-chlorophenyl)-2-(5,6-dimethoxybenzimidazol-1-yl)-1,3-thiazole-5-carboxylic acid Chemical compound C1=2C=C(OC)C(OC)=CC=2N=CN1C(SC=1C(O)=O)=NC=1C1=CC=CC(Cl)=C1 ASNYTHITDPHAHV-UHFFFAOYSA-N 0.000 claims description 10
• 125000004429 atom Chemical group 0.000 claims description 10
• 230000008569 process Effects 0.000 claims description 10
• 201000010099 disease Diseases 0.000 claims description 8
• 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 8
• 239000003814 drug Substances 0.000 claims description 8
• 125000001424 substituent group Chemical group 0.000 claims description 8
• UKLMWNNCZHYWNQ-UHFFFAOYSA-N 2-(5-methylbenzimidazol-1-yl)-4-phenyl-1,3-thiazole-5-carboxylic acid Chemical compound C1=NC2=CC(C)=CC=C2N1C(SC=1C(O)=O)=NC=1C1=CC=CC=C1 UKLMWNNCZHYWNQ-UHFFFAOYSA-N 0.000 claims description 7
• NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 7
• QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 7
• 229910052760 oxygen Inorganic materials 0.000 claims description 7
• 239000001301 oxygen Substances 0.000 claims description 7
• 229910052717 sulfur Inorganic materials 0.000 claims description 7
• 239000011593 sulfur Substances 0.000 claims description 7
• 238000004519 manufacturing process Methods 0.000 claims description 6
• 201000011510 cancer Diseases 0.000 claims description 5
• 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 5
• 150000002431 hydrogen Chemical class 0.000 claims description 5
• AYJRBUKJAAYPMJ-UHFFFAOYSA-N 2-(5,6-dimethoxybenzimidazol-1-yl)-4-phenyl-1,3-thiazole-5-carboxylic acid Chemical compound C1=2C=C(OC)C(OC)=CC=2N=CN1C(SC=1C(O)=O)=NC=1C1=CC=CC=C1 AYJRBUKJAAYPMJ-UHFFFAOYSA-N 0.000 claims description 4
• DMGNZHPEHRWPDM-UHFFFAOYSA-N 2-(7-hydroxybenzimidazol-1-yl)-4-phenyl-1,3-thiazole-5-carboxylic acid Chemical compound OC(=O)C=1SC(N2C3=C(O)C=CC=C3N=C2)=NC=1C1=CC=CC=C1 DMGNZHPEHRWPDM-UHFFFAOYSA-N 0.000 claims description 4
• NAOZLCIOJAYXIM-UHFFFAOYSA-N 2-(benzimidazol-1-yl)-4-phenyl-1,3-thiazole-5-carboxylic acid Chemical compound OC(=O)C=1SC(N2C3=CC=CC=C3N=C2)=NC=1C1=CC=CC=C1 NAOZLCIOJAYXIM-UHFFFAOYSA-N 0.000 claims description 4
• 125000003342 alkenyl group Chemical group 0.000 claims description 4
• 125000003785 benzimidazolyl group Chemical group N1=C(NC2=C1C=CC=C2)* 0.000 claims description 4
• 125000001072 heteroaryl group Chemical group 0.000 claims description 4
• 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 4
• LRXLYKKRELKYOF-UHFFFAOYSA-N 2-(4-carboxybenzimidazol-1-yl)-4-phenyl-1,3-thiazole-5-carboxylic acid Chemical compound OC(=O)C=1SC(N2C3=CC=CC(=C3N=C2)C(O)=O)=NC=1C1=CC=CC=C1 LRXLYKKRELKYOF-UHFFFAOYSA-N 0.000 claims description 3
• PNKPQBBBXKMHCY-UHFFFAOYSA-N 2-(4-hydroxybenzimidazol-1-yl)-4-phenyl-1,3-thiazole-5-carboxylic acid Chemical compound OC(=O)C=1SC(N2C3=CC=CC(O)=C3N=C2)=NC=1C1=CC=CC=C1 PNKPQBBBXKMHCY-UHFFFAOYSA-N 0.000 claims description 3
• IXIFALPWMQDPBP-UHFFFAOYSA-N 2-(5,6-dihydroxybenzimidazol-1-yl)-4-phenyl-1,3-thiazole-5-carboxylic acid Chemical compound OC(=O)C=1SC(N2C3=CC(O)=C(O)C=C3N=C2)=NC=1C1=CC=CC=C1 IXIFALPWMQDPBP-UHFFFAOYSA-N 0.000 claims description 3
• SRPRDOMMUDBFNU-UHFFFAOYSA-N 2-(5,6-dimethoxybenzimidazol-1-yl)-4-(1-methylindol-5-yl)-1,3-thiazole-5-carboxylic acid Chemical compound C1=C2N(C)C=CC2=CC(C=2N=C(SC=2C(O)=O)N2C=NC=3C=C(C(=CC=32)OC)OC)=C1 SRPRDOMMUDBFNU-UHFFFAOYSA-N 0.000 claims description 3
• YDQZCIGOVKGQCA-UHFFFAOYSA-N 2-(5,6-dimethoxybenzimidazol-1-yl)-4-(2-methylphenyl)-1,3-thiazole-5-carboxylic acid Chemical compound C1=2C=C(OC)C(OC)=CC=2N=CN1C(SC=1C(O)=O)=NC=1C1=CC=CC=C1C YDQZCIGOVKGQCA-UHFFFAOYSA-N 0.000 claims description 3
• RYGPCANKAYNMPZ-UHFFFAOYSA-N 2-(5,6-dimethoxybenzimidazol-1-yl)-4-(3-ethenylphenyl)-1,3-thiazole-5-carboxylic acid Chemical compound C1=2C=C(OC)C(OC)=CC=2N=CN1C(SC=1C(O)=O)=NC=1C1=CC=CC(C=C)=C1 RYGPCANKAYNMPZ-UHFFFAOYSA-N 0.000 claims description 3
• GESAUXAKNJZEKH-UHFFFAOYSA-N 2-(5,6-dimethoxybenzimidazol-1-yl)-4-(3-fluorophenyl)-1,3-thiazole-5-carboxylic acid Chemical compound C1=2C=C(OC)C(OC)=CC=2N=CN1C(SC=1C(O)=O)=NC=1C1=CC=CC(F)=C1 GESAUXAKNJZEKH-UHFFFAOYSA-N 0.000 claims description 3
• HLVGWBJEVPPBKB-UHFFFAOYSA-N 2-(5,6-dimethoxybenzimidazol-1-yl)-4-(3-methoxyphenyl)-1,3-thiazole-5-carboxylic acid Chemical compound COC1=CC=CC(C2=C(SC(=N2)N2C3=CC(OC)=C(OC)C=C3N=C2)C(O)=O)=C1 HLVGWBJEVPPBKB-UHFFFAOYSA-N 0.000 claims description 3
• SRWMWTKXCNSZLF-UHFFFAOYSA-N 2-(5,6-dimethoxybenzimidazol-1-yl)-4-(3-propan-2-ylphenyl)-1,3-thiazole-5-carboxylic acid Chemical compound C1=2C=C(OC)C(OC)=CC=2N=CN1C(SC=1C(O)=O)=NC=1C1=CC=CC(C(C)C)=C1 SRWMWTKXCNSZLF-UHFFFAOYSA-N 0.000 claims description 3
• YRSHBRPNANQIHZ-UHFFFAOYSA-N 2-(5,6-dimethoxybenzimidazol-1-yl)-4-(4-ethenylphenyl)-1,3-thiazole-5-carboxylic acid Chemical compound C1=2C=C(OC)C(OC)=CC=2N=CN1C(SC=1C(O)=O)=NC=1C1=CC=C(C=C)C=C1 YRSHBRPNANQIHZ-UHFFFAOYSA-N 0.000 claims description 3
• DJXMEFSAUOIGIZ-UHFFFAOYSA-N 2-(5,6-dimethoxybenzimidazol-1-yl)-4-(4-methoxyphenyl)-1,3-thiazole-5-carboxylic acid Chemical compound C1=CC(OC)=CC=C1C1=C(C(O)=O)SC(N2C3=CC(OC)=C(OC)C=C3N=C2)=N1 DJXMEFSAUOIGIZ-UHFFFAOYSA-N 0.000 claims description 3
• IHWFBJOKEWLGGY-UHFFFAOYSA-N 2-(5,6-dimethoxybenzimidazol-1-yl)-4-naphthalen-1-yl-1,3-thiazole-5-carboxylic acid Chemical compound C1=CC=C2C(C=3N=C(SC=3C(O)=O)N3C=NC=4C=C(C(=CC=43)OC)OC)=CC=CC2=C1 IHWFBJOKEWLGGY-UHFFFAOYSA-N 0.000 claims description 3
• GDFVHRAINCHFNY-UHFFFAOYSA-N 2-(5,6-dimethoxybenzimidazol-1-yl)-4-pyridin-3-yl-1,3-thiazole-5-carboxylic acid Chemical compound C1=2C=C(OC)C(OC)=CC=2N=CN1C(SC=1C(O)=O)=NC=1C1=CC=CN=C1 GDFVHRAINCHFNY-UHFFFAOYSA-N 0.000 claims description 3
• FRDRJZUWWFSZMH-UHFFFAOYSA-N 2-(5,6-dimethoxybenzimidazol-1-yl)-n,4-diphenyl-1,3-thiazole-5-carboxamide Chemical compound C1=2C=C(OC)C(OC)=CC=2N=CN1C(S1)=NC(C=2C=CC=CC=2)=C1C(=O)NC1=CC=CC=C1 FRDRJZUWWFSZMH-UHFFFAOYSA-N 0.000 claims description 3
• OLHHBNBLSWJMCJ-UHFFFAOYSA-N 2-(5-chloro-6-fluorobenzimidazol-1-yl)-4-phenyl-1,3-thiazole-5-carboxylic acid Chemical compound OC(=O)C=1SC(N2C3=CC(F)=C(Cl)C=C3N=C2)=NC=1C1=CC=CC=C1 OLHHBNBLSWJMCJ-UHFFFAOYSA-N 0.000 claims description 3
• RMLVXIDTNWGOGL-UHFFFAOYSA-N 2-(5-chloro-6-methylbenzimidazol-1-yl)-4-phenyl-1,3-thiazole-5-carboxylic acid Chemical compound C1=NC=2C=C(Cl)C(C)=CC=2N1C(SC=1C(O)=O)=NC=1C1=CC=CC=C1 RMLVXIDTNWGOGL-UHFFFAOYSA-N 0.000 claims description 3
• SEZLKARTIWTVRA-UHFFFAOYSA-N 2-(5-chlorobenzimidazol-1-yl)-4-phenyl-1,3-thiazole-5-carboxylic acid Chemical compound OC(=O)C=1SC(N2C3=CC=C(Cl)C=C3N=C2)=NC=1C1=CC=CC=C1 SEZLKARTIWTVRA-UHFFFAOYSA-N 0.000 claims description 3
• AWYDHHWUMSEDBL-UHFFFAOYSA-N 2-(6-chloro-5-methylbenzimidazol-1-yl)-4-phenyl-1,3-thiazole-5-carboxylic acid Chemical compound C1=2C=C(Cl)C(C)=CC=2N=CN1C(SC=1C(O)=O)=NC=1C1=CC=CC=C1 AWYDHHWUMSEDBL-UHFFFAOYSA-N 0.000 claims description 3
• YLWMPUZSBRYFED-UHFFFAOYSA-N 2-(6-chlorobenzimidazol-1-yl)-4-phenyl-1,3-thiazole-5-carboxylic acid Chemical compound OC(=O)C=1SC(N2C3=CC(Cl)=CC=C3N=C2)=NC=1C1=CC=CC=C1 YLWMPUZSBRYFED-UHFFFAOYSA-N 0.000 claims description 3
• HWJJDEHEYRTQDQ-UHFFFAOYSA-N 2-(8h-[1,3]dioxino[5,4-f]benzimidazol-3-yl)-4-phenyl-1,3-thiazole-5-carboxylic acid Chemical compound OC(=O)C=1SC(N2C3=CC=4OCOCC=4C=C3N=C2)=NC=1C1=CC=CC=C1 HWJJDEHEYRTQDQ-UHFFFAOYSA-N 0.000 claims description 3
• RWWYSPVYHFYQEI-UHFFFAOYSA-N 2-(benzimidazol-1-yl)-4-phenyl-1,3-thiazole-5-carboxamide Chemical compound NC(=O)C=1SC(N2C3=CC=CC=C3N=C2)=NC=1C1=CC=CC=C1 RWWYSPVYHFYQEI-UHFFFAOYSA-N 0.000 claims description 3
• QPEXOJRZKBRJKH-UHFFFAOYSA-N 4-(2,3-difluorophenyl)-2-(5,6-dimethoxybenzimidazol-1-yl)-1,3-thiazole-5-carboxylic acid Chemical compound C1=2C=C(OC)C(OC)=CC=2N=CN1C(SC=1C(O)=O)=NC=1C1=CC=CC(F)=C1F QPEXOJRZKBRJKH-UHFFFAOYSA-N 0.000 claims description 3
• DYUPBENDIHQGHP-UHFFFAOYSA-N 4-(2-chlorophenyl)-2-(5,6-dimethoxybenzimidazol-1-yl)-1,3-thiazole-5-carboxylic acid Chemical compound C1=2C=C(OC)C(OC)=CC=2N=CN1C(SC=1C(O)=O)=NC=1C1=CC=CC=C1Cl DYUPBENDIHQGHP-UHFFFAOYSA-N 0.000 claims description 3
• SCOSEDVZPKPHRX-UHFFFAOYSA-N 4-(3,4-dichlorophenyl)-2-(5,6-dimethoxybenzimidazol-1-yl)-1,3-thiazole-5-carboxylic acid Chemical compound C1=2C=C(OC)C(OC)=CC=2N=CN1C(SC=1C(O)=O)=NC=1C1=CC=C(Cl)C(Cl)=C1 SCOSEDVZPKPHRX-UHFFFAOYSA-N 0.000 claims description 3
• WLCMCUNZFGPDHY-UHFFFAOYSA-N 4-(3-chlorophenyl)-2-(5,6-dimethoxybenzimidazol-1-yl)-n'-(3-methylbenzoyl)-1,3-thiazole-5-carbohydrazide Chemical compound C1=2C=C(OC)C(OC)=CC=2N=CN1C(S1)=NC(C=2C=C(Cl)C=CC=2)=C1C(=O)NNC(=O)C1=CC=CC(C)=C1 WLCMCUNZFGPDHY-UHFFFAOYSA-N 0.000 claims description 3
• UULRFUVGBICGFR-UHFFFAOYSA-N 4-(3-chlorophenyl)-2-(5,6-dimethoxybenzimidazol-1-yl)-n'-(thiophene-2-carbonyl)-1,3-thiazole-5-carbohydrazide Chemical compound C1=2C=C(OC)C(OC)=CC=2N=CN1C(S1)=NC(C=2C=C(Cl)C=CC=2)=C1C(=O)NNC(=O)C1=CC=CS1 UULRFUVGBICGFR-UHFFFAOYSA-N 0.000 claims description 3
• NSPIHQBVBFUKPO-UHFFFAOYSA-N 4-(3-chlorophenyl)-2-(5,6-dimethoxybenzimidazol-1-yl)-n-(1,3-thiazol-2-yl)-1,3-thiazole-5-carboxamide Chemical compound C1=2C=C(OC)C(OC)=CC=2N=CN1C(S1)=NC(C=2C=C(Cl)C=CC=2)=C1C(=O)NC1=NC=CS1 NSPIHQBVBFUKPO-UHFFFAOYSA-N 0.000 claims description 3
• RJWVHJYICRWXSB-UHFFFAOYSA-N 4-(3-chlorophenyl)-2-(5,6-dimethoxybenzimidazol-1-yl)-n-pyrimidin-4-yl-1,3-thiazole-5-carboxamide Chemical compound C1=2C=C(OC)C(OC)=CC=2N=CN1C(S1)=NC(C=2C=C(Cl)C=CC=2)=C1C(=O)NC1=CC=NC=N1 RJWVHJYICRWXSB-UHFFFAOYSA-N 0.000 claims description 3
• 239000002671 adjuvant Substances 0.000 claims description 3
• 125000004093 cyano group Chemical group *C#N 0.000 claims description 3
• 125000000753 cycloalkyl group Chemical group 0.000 claims description 3
• 239000003937 drug carrier Substances 0.000 claims description 3
• RYVMXWTXDWJVDB-UHFFFAOYSA-N 2-(5,6-dimethoxybenzimidazol-1-yl)-4-(3,4-dimethoxyphenyl)-1,3-thiazole-5-carboxylic acid Chemical compound C1=C(OC)C(OC)=CC=C1C1=C(C(O)=O)SC(N2C3=CC(OC)=C(OC)C=C3N=C2)=N1 RYVMXWTXDWJVDB-UHFFFAOYSA-N 0.000 claims description 2
• SNWRTLGGPVJVQK-UHFFFAOYSA-N 2-(5,6-dimethoxybenzimidazol-1-yl)-4-(3-hydroxyphenyl)-1,3-thiazole-5-carboxylic acid Chemical compound C1=2C=C(OC)C(OC)=CC=2N=CN1C(SC=1C(O)=O)=NC=1C1=CC=CC(O)=C1 SNWRTLGGPVJVQK-UHFFFAOYSA-N 0.000 claims description 2
• YPENMNILWSQOND-UHFFFAOYSA-N 2-(5,6-dimethoxybenzimidazol-1-yl)-4-(4-methylphenyl)-1,3-thiazole-5-carboxylic acid Chemical compound C1=2C=C(OC)C(OC)=CC=2N=CN1C(SC=1C(O)=O)=NC=1C1=CC=C(C)C=C1 YPENMNILWSQOND-UHFFFAOYSA-N 0.000 claims description 2
• PHUBUICFEOKUND-UHFFFAOYSA-N 2-(5,6-dimethoxybenzimidazol-1-yl)-4-[3-(dimethylcarbamoyl)phenyl]-1,3-thiazole-5-carboxylic acid Chemical compound C1=2C=C(OC)C(OC)=CC=2N=CN1C(SC=1C(O)=O)=NC=1C1=CC=CC(C(=O)N(C)C)=C1 PHUBUICFEOKUND-UHFFFAOYSA-N 0.000 claims description 2
• GCBRNDVJHYCXHT-UHFFFAOYSA-N 2-(5,6-dimethoxybenzimidazol-1-yl)-4-[3-(trifluoromethyl)phenyl]-1,3-thiazole-5-carboxylic acid Chemical compound C1=2C=C(OC)C(OC)=CC=2N=CN1C(SC=1C(O)=O)=NC=1C1=CC=CC(C(F)(F)F)=C1 GCBRNDVJHYCXHT-UHFFFAOYSA-N 0.000 claims description 2
• KKSARMOSVBRKOK-UHFFFAOYSA-N 2-(5,6-dimethoxybenzimidazol-1-yl)-4-phenyl-5-(2h-tetrazol-5-yl)-1,3-thiazole Chemical compound C1=2C=C(OC)C(OC)=CC=2N=CN1C(S1)=NC(C=2C=CC=CC=2)=C1C1=NN=NN1 KKSARMOSVBRKOK-UHFFFAOYSA-N 0.000 claims description 2
• DATNXVFSSNJTPA-UHFFFAOYSA-N 2-(5,6-dimethoxybenzimidazol-1-yl)-4-thiophen-3-yl-1,3-thiazole-5-carboxylic acid Chemical compound C1=2C=C(OC)C(OC)=CC=2N=CN1C(SC=1C(O)=O)=NC=1C=1C=CSC=1 DATNXVFSSNJTPA-UHFFFAOYSA-N 0.000 claims description 2
• JGFXBKCPGKLGOC-UHFFFAOYSA-N 2-(5,6-dimethoxybenzimidazol-1-yl)-n,n-dimethyl-4-phenyl-1,3-thiazole-5-carboxamide Chemical compound C1=2C=C(OC)C(OC)=CC=2N=CN1C(SC=1C(=O)N(C)C)=NC=1C1=CC=CC=C1 JGFXBKCPGKLGOC-UHFFFAOYSA-N 0.000 claims description 2
• LSPBWHHLSDAMJA-UHFFFAOYSA-N 2-(5,6-dimethoxybenzimidazol-1-yl)-n-ethyl-4-phenyl-1,3-thiazole-5-carboxamide Chemical compound CCNC(=O)C=1SC(N2C3=CC(OC)=C(OC)C=C3N=C2)=NC=1C1=CC=CC=C1 LSPBWHHLSDAMJA-UHFFFAOYSA-N 0.000 claims description 2
• YLSWRBTYBDZDEY-UHFFFAOYSA-N 2-(5,6-dimethylbenzimidazol-1-yl)-4-phenyl-1,3-thiazole-5-carboxylic acid Chemical compound C1=2C=C(C)C(C)=CC=2N=CN1C(SC=1C(O)=O)=NC=1C1=CC=CC=C1 YLSWRBTYBDZDEY-UHFFFAOYSA-N 0.000 claims description 2
• UEGUPKZLQHKAKO-UHFFFAOYSA-N 2-(5-methoxy-6-methylbenzimidazol-1-yl)-4-phenyl-1,3-thiazole-5-carboxylic acid Chemical compound C1=2C=C(C)C(OC)=CC=2N=CN1C(SC=1C(O)=O)=NC=1C1=CC=CC=C1 UEGUPKZLQHKAKO-UHFFFAOYSA-N 0.000 claims description 2
• ZMGWBKZUFTUTEA-UHFFFAOYSA-N 2-(6-chloro-5-fluorobenzimidazol-1-yl)-4-phenyl-1,3-thiazole-5-carboxylic acid Chemical compound OC(=O)C=1SC(N2C3=CC(Cl)=C(F)C=C3N=C2)=NC=1C1=CC=CC=C1 ZMGWBKZUFTUTEA-UHFFFAOYSA-N 0.000 claims description 2
• QLMZHYHCYBJJRB-UHFFFAOYSA-N 2-(6-methoxy-5-methylbenzimidazol-1-yl)-4-phenyl-1,3-thiazole-5-carboxylic acid Chemical compound C1=NC=2C=C(C)C(OC)=CC=2N1C(SC=1C(O)=O)=NC=1C1=CC=CC=C1 QLMZHYHCYBJJRB-UHFFFAOYSA-N 0.000 claims description 2
• OCNNMZSXISRRDO-UHFFFAOYSA-N 2-[5,6-bis(2-methoxyethoxy)benzimidazol-1-yl]-4-phenyl-1,3-thiazole-5-carboxylic acid Chemical compound C1=2C=C(OCCOC)C(OCCOC)=CC=2N=CN1C(SC=1C(O)=O)=NC=1C1=CC=CC=C1 OCNNMZSXISRRDO-UHFFFAOYSA-N 0.000 claims description 2
• BLJVEZPCIIAHTC-UHFFFAOYSA-N 2-[6-(2-methoxyethoxy)benzimidazol-1-yl]-4-phenyl-1,3-thiazole-5-carboxylic acid Chemical compound C12=CC(OCCOC)=CC=C2N=CN1C(SC=1C(O)=O)=NC=1C1=CC=CC=C1 BLJVEZPCIIAHTC-UHFFFAOYSA-N 0.000 claims description 2
• PQSSBTQHZHXLJL-UHFFFAOYSA-N 4-(1,3-benzodioxol-5-yl)-2-(5,6-dimethoxybenzimidazol-1-yl)-1,3-thiazole-5-carboxylic acid Chemical compound C1=C2OCOC2=CC(C=2N=C(SC=2C(O)=O)N2C=NC=3C=C(C(=CC=32)OC)OC)=C1 PQSSBTQHZHXLJL-UHFFFAOYSA-N 0.000 claims description 2
• DUVUPQWKKQCZJX-UHFFFAOYSA-N 4-(2,3-dihydro-1,4-benzodioxin-6-yl)-2-(5,6-dimethoxybenzimidazol-1-yl)-1,3-thiazole-5-carboxylic acid Chemical compound O1CCOC2=CC(C=3N=C(SC=3C(O)=O)N3C=NC=4C=C(C(=CC=43)OC)OC)=CC=C21 DUVUPQWKKQCZJX-UHFFFAOYSA-N 0.000 claims description 2
• RJXKNTHXJWTEPR-UHFFFAOYSA-N 4-(2-chloropyridin-4-yl)-2-(5,6-dimethoxybenzimidazol-1-yl)-1,3-thiazole-5-carboxylic acid Chemical compound C1=2C=C(OC)C(OC)=CC=2N=CN1C(SC=1C(O)=O)=NC=1C1=CC=NC(Cl)=C1 RJXKNTHXJWTEPR-UHFFFAOYSA-N 0.000 claims description 2
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